References
-
1.
Akay HO, Kervancioglu M, Nazaroglu H, Katar S, Ozmen CA, Kilinc I, et al. Horseshoe lung associated with rare bilateral variant of scimitar syndrome: demonstration by 64-slice MDCT angiography. Pediatr Radiol. 2008;38(5):563-6. [PubMed ID: 18189131]. https://doi.org/10.1007/s00247-007-0722-8.
-
2.
Basson CT, Solomon SD, Weissman B, MacRae CA, Poznanski AK, Prieto F, et al. Genetic heterogeneity of heart-hand syndromes. Circulation. 1995;91(5):1326-9. [PubMed ID: 7867169].
-
3.
Salerno T, Guccione P, Malena S, Cutrera R. Horseshoe lung associated with unique left pulmonary vein: an unreported association. Pediatr Cardiol. 2010;31(6):905-7. [PubMed ID: 20512320]. https://doi.org/10.1007/s00246-010-9735-4.
-
4.
Oguz B, Alan S, Ozcelik U, Haliloglu M. Horseshoe lung associated with left-lung hypoplasia, left pulmonary artery sling and bilateral agenesis of upper lobe bronchi. Pediatr Radiol. 2009;39(9):1002-5. [PubMed ID: 19458945]. https://doi.org/10.1007/s00247-009-1300-z.
-
5.
McDermott DA, Bressan MC, He J, Lee JS, Aftimos S, Brueckner M, et al. TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome. Pediatr Res. 2005;58(5):981-6. [PubMed ID: 16183809].
-
6.
Caglayan AO, Koklu E, Saatci C, Gunes T, Ozkul Y, Narin N, et al. Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2). Ann Saudi Med. 2008;28(3):209-12. [PubMed ID: 18500176].
-
7.
Gonzalez Espinosa C, Artiles Perez L, Garcia Baez M, Otero Gomez A, Garcia Miranda JL. [Holt-Oram syndrome with chromosomopathy (author's transl)]. An Esp Pediatr. 1982;16(1):77-81. [PubMed ID: 7081854].
-
8.
Le Meur N, Goldenberg A, Michel-Adde C, Drouin-Garraud V, Blaysat G, Marret S, et al. Molecular characterization of a 14q deletion in a boy with features of Holt-Oram syndrome. Am J Med Genet A. 2005;134(4):439-42. [PubMed ID: 15810003]. https://doi.org/10.1002/ajmg.a.30660.
-
9.
Tseng YR, Su YN, Lu FL, Jeng SF, Hsieh WS, Chen CY, et al. Holt-Oram syndrome with right lung agenesis caused by a de novo mutation in the TBX5 gene. Am J Med Genet A. 2007;143A(9):1012-4. [PubMed ID: 17366586]. https://doi.org/10.1002/ajmg.a.31672.
-
10.
Begemann G, Ingham PW. Developmental regulation of Tbx5 in zebrafish embryogenesis. Mech Dev. 2000;90(2):299-304. [PubMed ID: 10640716].
-
11.
Tiozzo C, De Langhe S, Carraro G, Alam DA, Nagy A, Wigfall C, et al. Fibroblast growth factor 10 plays a causative role in the tracheal cartilage defects in a mouse model of Apert syndrome. Pediatr Res. 2009;66(4):386-90. [PubMed ID: 19581825]. https://doi.org/10.1203/PDR.0b013e3181b45580.